Canonical Allele Identifier: CA513349419
Community Standard Title: NM_020070.4(IGLL1):c.117G>A (p.Leu39=)
Gene: IGLL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23580074C>T , CM000684.2:g.23580074C>T GRCh38
NC_000022.10:g.23922261C>T , CM000684.1:g.23922261C>T GRCh37
NC_000022.9:g.22252261C>T NCBI36
NG_009791.1:g.5235G>A , LRG_69:g.5235G>A

Transcript Alleles

HGVS Amino-acid Change
NM_020070.4:c.117G>A MANE Select NP_064455.1:p.Leu39=
ENST00000330377.3:c.117G>A MANE Select ENSP00000329312.2:p.Leu39=
NM_001369906.1:c.117G>A NP_001356835.1:p.Leu39=
NM_020070.3:c.117G>A NP_064455.1:p.Leu39=
NM_152855.2:c.117G>A NP_690594.1:p.Leu39=
NM_152855.3:c.117G>A NP_690594.1:p.Leu39=
ENST00000249053.3:c.117G>A ENSP00000249053.3:p.Leu39=
ENST00000330377.2:c.117G>A ENSP00000329312.2:p.Leu39=
ENST00000438703.1:c.117G>A ENSP00000403391.1:p.Leu39=
XM_011530169.1:c.117G>A XP_011528471.1:p.Leu39=
XM_011530169.2:c.117G>A XP_011528471.1:p.Leu39=